Do not administer if the substance is not known to be absorbed by activated charcoal.
Corrosive ingestion as it can obscure endoscopy.
Seizures.
Associated Protocols:
Activated charcoal may only be given by order of medical command or poison control.
Adenosine
Class: Antiarrhythmic
Indications:
Narrow complex REGULAR supraventricular tachycardia refractory to vagal maneuvers.
Mechanism of Action:
Slows conduction through AV node; interrupts re-entrant pathways; chemically cardioverts.
It is naturally occurring in all cells, a byproduct of ATP breakdown.
Adenosine receptors located in lungs and cardiomyocytes stimulate decreased electrical conduction, decreased SA node automaticity, and slower conduction velocity.
Dose:
Adult:
Attempt vagal maneuvers first.
6mg (2cc) IV rapidly over 1-3 seconds, flush with 20cc NS bolus.
May repeat 12mg bolus once more in 2 minutes.
3rd dose of 12mg requires medical command prior to administration.
Acts as a noncompetitive alpha and beta adrenergic inhibitor; delays repolarization and increases action potential duration.
Dose:
VF/VT (pulseless): 300mg IV/IO; may repeat 150mg IV/IO in 10 minutes.
Stable Irregular Narrow Complex Tachycardia or Stable VT/Wide complex with a pulse: 150mg in 50-100ml NS over 10 minutes.
Recurrent VT or Runs of VT post-ROSC: 1mg/min infusion (Max 2.2g in 24hrs).
Pediatric:
VT (Pulsed) and SVT: 5mg/kg in 50ml NS over 20-60 minutes.
VF/VT (Pulseless): 5mg/kg IV/IO (Max 300mg).
Side Effects:
Vasodilation, low BP, low HR, AV block, hepatotoxicity, Torsades, CHF.
Contraindications:
Known hypersensitivity, iodine hypersensitivity, bradycardia, AV block > 1 degree without a pacemaker, hypotension (SBP < 100 mmHg).
Associated Protocols:
3031A/P, 3080, 5022P, 5023A & P
Ancef (Cefazolin)
Class: Cephalosporin antibiotic
Indications:
Open fractures, amputations.
Mechanism of Action:
Inhibits bacterial cell wall synthesis leading to cell death.
Dose:
Adult (>50kg): 2g IV/IO.
Peds (9 to ≤14 years old, 30-50kg): 1g IV/IO.
Side Effects:
Nausea, vomiting, diarrhea, headaches.
Contraindications:
Hypersensitivity, allergic to cephalosporins or penicillin.
Associated Protocols:
6093
Aspirin
Class: Antiplatelet/NSAID
Indications:
Chest pain, acute myocardial infarctions, mild to moderate pain in adults.
Mechanism of Action:
Blocks formation of thromboxane A2, limiting platelet aggregation and arterial constriction.
Decreases levels of PGE2, reducing pain and inflammation.
Dose:
324mg (4 pills) PO (chewed).
650mg PO (>14 years old).
Side Effects:
GI bleeding.
Contraindications:
Gastrointestinal bleeding, active ulcer disease, hemorrhagic stroke, bleeding disorders, children with chickenpox or flu-like symptoms, known hypersensitivity.
Intracranial/intraspinal hemorrhage, delirium tremens, solution not clear, seals not intact, known or suspected stroke without hypoglycemia.
Associated Protocols:
3080, 6081, 7002, 7006, 7007
Diazepam (Valium)
Class: Benzodiazepine
Indications:
Major motor seizures; status epilepticus; premedication prior to cardioversion; acute anxiety.
Mechanism of Action:
Benzodiazepines bind to GABA type A receptors in the brain, potentiating the inhibitory effect of GABA, thus providing sedation, skeletal muscle relaxation, and anticonvulsant activity.
Dose:
Seizures:
Adult: 0.2mg/kg (max 10mg IV/IO), may repeat every 5 minutes until max of 0.6mg/kg.
Pediatric: 0.3mg/kg IV/IO/IM (max 5mg), may repeat every 5 minutes until max of 0.6mg/kg.
Sedation: 5-10mg IV/IO (0.1mg/kg) titrated slowly, may repeat every 5 minutes until max of 0.3mg/kg.
Behavioral: (IMCRASS 2) 0.05mg/kg IM (max 5mg). (IMCRASS 3-4) Double if no midazolam available.
Contact Command if possible: Reduce dose for >65 years.
Histamine receptor blocker, reducing bronchoconstriction and vasodilation.
Dose:
Adult: 50mg IV/IM/IO/PO.
Peds: 1mg/kg IV/IO/IM/PO (max 50mg).
Side Effects:
Drowsiness, sedation, seizures.
Contraindications:
Acute asthma (thickens secretions); patients with cardiac histories; known sensitivity, patients taking MAO inhibitors; newborns/nursing mothers.
Associated Protocols:
4011
Dobutamine
Class: Adrenergic Inotropic Agent
Indications:
CHF with cardiogenic shock (SBP 70-90 mmHg), post-ROSC hypotension.
Mechanism of Action:
Beta-1 agonist with positive inotropic effects, increasing cardiac contractility and stroke volume; mild beta-2 agonist.
Dose:
5-20 mcg/kg/min; start at 5mcg/kg/min, increase every 10 minutes by 5mcg/kg/min until SBP >100mmHg.
Side Effects:
Angina, PVCs, tachydysrhythmia.
Contraindications:
Hypersensitivity, hypovolemia.
Associated Protocols:
5002
Dopamine
Class: Inotropic, Vasopressor
Indications:
Cardiogenic and septic shock; hypotension with low cardiac output.
Mechanism of Action:
Stimulates alpha and beta adrenergic receptors.
Moderate doses stimulate B1, increasing inotropic effects and cardiac output; higher doses cause vasoconstriction (alpha dominance).
Dose:
Start at 5mcg/kg/min, increase every 10 minutes by 5mcg/kg/min until SBP >100mmHg.
(>120mmHg in ROSC or [70+(age x 2)] in children)
DO NOT exceed 20mcg/kg/min unless ordered by medical command physician.
Side Effects:
Headache, anxiety, dyspnea, dysrhythmias.
Contraindications:
Pheochromocytoma, VF, VT, or other ventricular arrhythmias; known sensitivity (including sulfites).
Correct hypovolemia with fluid replacement before administering dopamine; trauma.
Associated Protocols:
3000A, 3080, 5002, 5021A & P, 6002, 7005
Droperidol
Class: Antiemetic/Antipsychotic
Indications:
Nausea and vomiting; excited delirium/psychosis; need for chemical restraint.
Mechanism of Action:
Reduces motor activity, anxiety, and causes sedation; blocks dopamine receptors in chemoreceptor trigger zone (anti-emetic property); binds to postsynaptic GABA receptors in the CNS, enhancing the inhibitory effect of GABA, leading to sedation and anti-anxiety activities.
Dose:
Adult: 1.25mg IV/IO/IM (nausea).
If >65 years or <60 kg, 0.625mg, may repeat after 15 minutes.
Blocks the conversion of Angiotensin I to Angiotensin II, decreasing systemic vascular resistance, preload, and afterload. Reduces sodium and water retention.
Dose:
0.625-1.25mg IV or 25mg SL.
Side Effects:
Syncope, tachycardia, hypotension, arthralgia, rash, fever, risk of hyperkalemia with DM and renal disease.
Contraindications:
Known hypersensitivity or allergy to ACE inhibitors.
Associated Protocols:
5002
Epinephrine 1mg/ml (Formerly 1:1000)
Class: Non-Selective Beta Agonist
Indications:
Severe anaphylaxis; asthma (bronchospasm) needing medical command.
Mechanism of Action:
Catecholamine with strong alpha adrenergic, strong beta-1, and moderate beta-2 effects.
Caution in patients with known cardiovascular disease or >45 years; hypertension, cerebrovascular disease; shock from causes other than anaphylactic shock; closed-angle glaucoma; diabetes; pregnant women in active labor; known sensitivity to epinephrine or sulfites.
Associated Protocols:
4011, 4022, 4023
Epinephrine 0.1mg/ml (Formerly 1:10,000)
Class: Vasopressor
Indications:
Cardiac arrest.
Mechanism of Action:
Catecholamine with strong alpha adrenergic, strong beta-1, and moderate beta-2 effects.
Alpha stimulation results in systemic vasoconstriction, increasing peripheral vascular resistance.
Arrhythmias other than VF, asystole, PEA; cardiovascular disease; hypertension; cerebrovascular disease; shock from causes other than anaphylactic shock; closed-angle glaucoma; diabetes; pregnant women in active labor; known sensitivity to epinephrine or sulfites; caution in patients >45 years.
Associated Protocols:
3000A, 3031, 3032, 3033, 3080, 5021, 6002, 7005
Etomidate
Class: Hypnotic
Indications:
Sedation-assisted intubation.
Mechanism of Action:
Exact action unknown, appears to have GABA-like effects.
Known hypersensitivity to drug, other sympathomimetics, or peanuts. MAOI use within 14 days, angioedema, tachydysrhythmias, severe cardiac disease. Caution with drugs that prolong QT interval.
Associated Protocols:
4022, 4023, 4011
Levophed (Norepinephrine)
Class: Adrenergic receptor agonist
Indications:
Non-hypovolemic shock/hypotension.
Mechanism of Action:
Norepinephrine acts on α1, β1, and β2 receptors with the strongest α1 activity leading to vasoconstriction, with moderate β1 receptor activity contributing to cardiac stimulation.
Dose:
0.05-0.5 mcg/kg/min, increasing by 0.05 mcg/kg/min every 5 minutes to a MAP of 65 mmHg.
Side Effects:
Hypertension, reflex bradycardia, mesenteric or peripheral ischemia.
Contraindications:
Sulfite allergy.
Associated Protocols:
6002, 3080
Lactated Ringers
Class: Isotonic Crystalloid
Indications:
Hypovolemic shock; burns; dehydration.
Mechanism of Action:
Replaces water and electrolytes; contains 600mg NaCl, 310mg Na Lactate, 30mg KCl, and chloride dehydrate.
Dose:
IV/IO dose depends on patient condition and treatment situation.
Side Effects:
Rare.
Contraindications:
Metabolic acidosis or alkalosis, severe liver disease, or anoxic states.
Associated Protocols:
Lidocaine 2%
Class: Antiarrhythmic
Indications:
V-Fib or pulseless V-Tach; wide complex tachycardia with pulses; control of ventricular arrhythmias (PVCs).
Mechanism of Action:
Decreases automaticity; combines with fast sodium channels, inhibiting recovery after repolarization, decreasing myocardial excitability and conduction velocity.
IO Anesthetic: 0.5mg/kg slow push up to 40mg.
Dose:
For cardiac arrest VT/VF: 1.5mg/kg IV/IO; repeat 0.5-0.75mg/kg every 5-10 mins (total max dose of 3mg/kg).
For wide complex tachycardia: Adults 1.5mg/kg IVP; repeat 0.75mg/kg IV/IO after contacting medical command; or after ROSC start a drip of 2-4 mg/min.
For pediatric: 1mg/kg IV/IO (max 3mg/kg).
Side Effects:
Seizures, slurred speech, altered mental status.
Contraindications:
Thrombocytopenia, known sensitivity to lidocaine, sulfite, or paraben.
Use with caution in bradycardia, hypovolemia, cardiogenic shock, Adams-Stokes syndrome, Wolff-Parkinson-White syndrome.
Associated Protocols:
1000, 3031, 3032, 3080, 5023
Lorazepam (Ativan)
Class: Benzodiazepine
Indications:
Severe anxiety; seizures; status epilepticus; sedation.
Mechanism of Action:
Benzodiazepines bind to GABA type A receptors, enhancing GABA activity, producing CNS depression as required (sedation, muscle relaxation, anticonvulsant activity).
Suppresses seizure activity from cortical, thalamic, and limbic areas.
Dose:
Adult: 1-2mg IV/IO/IM/Intranasal (0.1mg/kg - max 2mg per dose); may repeat every 5 minutes up to max 4mg.
Behavioral: contact command if possible reduce dose in half for patients >65.
Cushing syndrome, fungal infection, measles, varicella, known sensitivity (including sulfites).
Use with caution in active infections, renal disease, diabetes, penetrating spinal cord injury; hypertension, seizures, CHF; caution in GI bleeding patients.
Respiratory depression, shock, known sensitivity; caution in hypotension, acute bronchial asthma, respiratory insufficiency, head trauma, RV infarct MI.
Associated Protocols:
5001, 6003, 6071
Naloxone (Narcan)
Class: Narcotic Antagonist
Indications:
Narcotic overdose (respiratory depression), alcohol induced coma, coma of unknown origin.
Mechanism of Action:
Reverses respiratory depression due to opiate drugs; competitively inhibits narcotic receptor sites.
Dose:
Adult: 0.4mg titrate to effect (max 2mg IV/IO); IM/Intranasal: max 2mg.
Pediatric: 0.1mg/kg IV/IO/IM/IN (max 0.4mg).
Side Effects:
Withdrawal symptoms in addicted patients (tremors, increased BP); if too rapid reversal: nausea, vomiting, sweating, tachycardia.
Contraindications:
Known sensitivity to naloxone, nalmefene, or naltrexone; caution in patients with supraventricular arrhythmias or other cardiac disease, head trauma, or brain tumor.
Associated Protocols:
3031, 4001, 4002, 6003, 6071, 7002
Nitroglycerin
Class: Nitrate
Indications:
CHF to decrease pulmonary venous congestion and improve cardiac output; suspected acute coronary syndrome (chest pain).
Mechanism of Action:
Smooth muscle relaxant acting on vascular, bronchial, uterine, intestinal smooth muscle; reduces preload during acute pulmonary edema.
Dose:
Chest Pain: 1 tablet or spray sublingually every 5 minutes (max of 3). Systolic BP must be over 100 mmHg.
CHF Dosage: repeat every 3-5 minutes as long as BP >100 mmHg; after initial dose give based on SBP: 3 SL tablets or spray (if SBP >180), 2 SL tablets or sprays (if SBP 140-180), 1 SL tablet or spray (if SBP 100-140).
IV: (Drip or Push Dose): Optional: 200 mcg slow IV push over 2 mins; repeat up to 3 doses or
with IV Pump: 5-200 mcg/min titrated to systolic >100.
Side Effects:
Headache, hypotension, syncope, tachycardia, flushing, burning under tongue.
Contraindications:
Hypotension, severe bradycardia, or tachycardia; right-sided MI; increased intracranial pressure; intracranial bleeding; patients on erectile dysfunction medications (Viagra, Cialis, Levitra); known sensitivity to nitrates.
Ensure no additional fetus is present and the placenta has been delivered prior to administration.
Associated Protocols:
7087
Pralidoxime Chloride (2PAMCl)
Class: Cholinesterase Reactivator
Indications:
Organophosphate or nerve agent poisoning.
Mechanism of Action:
Administered with atropine; attaches to anionic site of the enzyme, having a higher affinity for phosphorylation than the enzyme itself, enabling the enzyme activation.
Pulmonary congestion, pulmonary edema, known sensitivity.
Associated Protocols:
Sodium Thiosulfate
Class: Antidote
Indications:
Cyanide toxicity.
Mechanism of Action:
Donates sulfur atom required to transform cyanomethemoglobin to thiocyanate, thus detoxifying cyanide.
Cyanide binds to ferric iron in the cytochrome oxidase system, disrupting oxidative phosphorylation and causing shift to anaerobic metabolism, leading to metabolic acidosis.
Dose:
Adult: 12.5 grams (50 ml) IV/IO over 1-2 minutes.
Pediatric: 1.6ml/kg IV/IO over 1-2 minutes (max dose 12.5 grams).
Side Effects:
Nausea/vomiting, headache, hypotension.
Contraindications:
None; precaution noted against concurrent administration with hydroxocobalamin.
Associated Protocols:
8031, 8081
Tetracaine 0.5% Ophthalmic Solution
Class: Local anesthetic (ester group)
Indications:
Corneal abrasion or injury.
Mechanism of Action:
Blocks sodium ion channels required for initiating and conducting neuronal impulses, achieving corneal local anesthesia within 10-20 seconds, lasting 10-20 minutes.
Dose:
Adult: 2 drops in affected eye.
Side Effects:
Burning, conjunctival redness, ocular discomfort.
Contraindications:
None noted.
Associated Protocols:
8031
Terbutaline
Class: Selective Beta-2 agonist
Indications:
Bronchospasm.
Mechanism of Action:
Stimulates beta-2 receptors causing relaxation of bronchial smooth muscle and prompt bronchodilation.
Blocks effects of COX-1 and COX-2 enzymes, which are key to making prostaglandins, reducing PG production and associated effects.
Dose:
15mg IV/IO (30mg IM); preferred IV if kidney stone suspected (Peds ≥2y/o: 0.5mg/kg IV/IO/IM, max 15mg IV/IO or 30mg IM).
Note:
NSAIDs contraindicated if an oral NSAID taken in the last 6 hours; or history of bleeding/suspected bleeding (external/internal trauma, GI, vascular); known kidney disease/failure or kidney transplant.
History of peptic ulcer disease/GI bleeds; renal insufficiency; hypovolemic patients; pregnancy (third trimester); nursing mothers; known allergy to ASA or other NSAIDs; stroke/suspected stroke; need for major surgery in the immediate future.
Associated Protocols:
6003, 7003
Tranexamic Acid
Class: Coagulation modifier, Antifibrinolytic
Indications:
Traumatic bleeding.
Mechanism of Action:
Synthetic derivative of lysine inhibiting fibrinolysis by blocking lysine binding sites on plasminogen, preventing clot breakdown.
Additional mechanisms including decreasing inflammatory responses to trauma are under exploration.
Dose:
1g over 10 minutes (1g/100ml NSS).
Side Effects:
Hypotension, nausea/vomiting, diarrhea.
Contraindications:
Do not use with blood products or penicillin in the same IV/IO line.
Associated Protocols:
6094
Verapamil
Class: Calcium Channel Blocker
Indications:
PSVT refractory to adenosine; narrow complex IRREGULAR SVT (needs command); adenosine-refractory REGULAR SVT; AFib with rapid ventricular response; atrial flutter.
Mechanism of Action:
Causes vascular dilation and slows conduction through the AV node; inhibits re-entry dysrhythmias such as PSVT.
Decreases myocardial oxygen demand due to inotropic effects.
Dose:
5mg IV over 2-3 minutes; repeat 5-10mg in 15 minutes.